Canonical Allele Identifier: CA467781349
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130910T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255523T>C , CM000671.2:g.133255523T>C GRCh38
NC_000009.11:g.136130910T>C , CM000671.1:g.136130910T>C GRCh37
NC_000009.10:g.135120731T>C NCBI36
NG_006669.1:g.22145A>G
NG_006669.2:g.24693A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1237A>G
ENST00000647353.1:n.54-4371A>G
ENST00000679909.1:c.28+19639A>G ENSP00000506089.1:n.28+19639A>G
ENST00000453660.3:n.1219A>G
ENST00000611156.4:c.*143A>G ENSP00000483265.1:n.*143A>G
NM_020469.2:c.*143A>G NP_065202.2:n.*143A>G
NM_020469.3:c.*143A>G NP_065202.2:n.*143A>G
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